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Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues

BACKGROUND: As a result of the epigenetic phenomenon of X chromosome inactivation (XCI) every woman is a mosaic of cells with either an inactive paternal X chromosome or an inactive maternal X chromosome. The ratio between inactive paternal and maternal X chromosomes is different for every female in...

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Autores principales: de Hoon, Bas, Monkhorst, Kim, Riegman, Peter, Laven, Joop S E, Gribnau, Joost
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4680131/
https://www.ncbi.nlm.nih.gov/pubmed/26220467
http://dx.doi.org/10.1136/jmedgenet-2015-103194
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author de Hoon, Bas
Monkhorst, Kim
Riegman, Peter
Laven, Joop S E
Gribnau, Joost
author_facet de Hoon, Bas
Monkhorst, Kim
Riegman, Peter
Laven, Joop S E
Gribnau, Joost
author_sort de Hoon, Bas
collection PubMed
description BACKGROUND: As a result of the epigenetic phenomenon of X chromosome inactivation (XCI) every woman is a mosaic of cells with either an inactive paternal X chromosome or an inactive maternal X chromosome. The ratio between inactive paternal and maternal X chromosomes is different for every female individual, and can influence an X-encoded trait or disease. A multitude of X linked conditions is known, and for many of them it is recognised that the phenotype in affected female carriers of the causative mutation is modulated by the XCI ratio. To predict disease severity an XCI ratio is usually determined in peripheral blood samples. However, the correlation between XCI ratios in peripheral blood and disease affected tissues, that are often inaccessible, is poorly understood. Here, we tested several tissues obtained from autopsies of 12 female individuals for patch size and XCI ratio. METHODS: XCI ratios were analysed using methyl-sensitive PCR-based assays for the AR, PCSK1N and SLITRK4 loci. XCI patch size was analysed by testing the XCI ratio of tissue samples with decreasing size. RESULTS: XCI patch size was analysed for liver, muscle, ovary and brain samples and was found too small to confound testing for XCI ratio in these tissues. XCI ratios were determined in the easily accessible tissues, blood, buccal epithelium and hair follicle, and compared with ratios in several inaccessible tissues. CONCLUSIONS: Buccal epithelium is preferable over peripheral blood for predicting XCI ratios of inaccessible tissues. Ovary is the only inaccessible tissue showing a poor correlation to blood and buccal epithelium, but has a good correlation to hair follicle instead.
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spelling pubmed-46801312015-12-18 Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues de Hoon, Bas Monkhorst, Kim Riegman, Peter Laven, Joop S E Gribnau, Joost J Med Genet Epigenetics BACKGROUND: As a result of the epigenetic phenomenon of X chromosome inactivation (XCI) every woman is a mosaic of cells with either an inactive paternal X chromosome or an inactive maternal X chromosome. The ratio between inactive paternal and maternal X chromosomes is different for every female individual, and can influence an X-encoded trait or disease. A multitude of X linked conditions is known, and for many of them it is recognised that the phenotype in affected female carriers of the causative mutation is modulated by the XCI ratio. To predict disease severity an XCI ratio is usually determined in peripheral blood samples. However, the correlation between XCI ratios in peripheral blood and disease affected tissues, that are often inaccessible, is poorly understood. Here, we tested several tissues obtained from autopsies of 12 female individuals for patch size and XCI ratio. METHODS: XCI ratios were analysed using methyl-sensitive PCR-based assays for the AR, PCSK1N and SLITRK4 loci. XCI patch size was analysed by testing the XCI ratio of tissue samples with decreasing size. RESULTS: XCI patch size was analysed for liver, muscle, ovary and brain samples and was found too small to confound testing for XCI ratio in these tissues. XCI ratios were determined in the easily accessible tissues, blood, buccal epithelium and hair follicle, and compared with ratios in several inaccessible tissues. CONCLUSIONS: Buccal epithelium is preferable over peripheral blood for predicting XCI ratios of inaccessible tissues. Ovary is the only inaccessible tissue showing a poor correlation to blood and buccal epithelium, but has a good correlation to hair follicle instead. BMJ Publishing Group 2015-11 2015-07-28 /pmc/articles/PMC4680131/ /pubmed/26220467 http://dx.doi.org/10.1136/jmedgenet-2015-103194 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epigenetics
de Hoon, Bas
Monkhorst, Kim
Riegman, Peter
Laven, Joop S E
Gribnau, Joost
Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues
title Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues
title_full Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues
title_fullStr Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues
title_full_unstemmed Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues
title_short Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues
title_sort buccal swab as a reliable predictor for x inactivation ratio in inaccessible tissues
topic Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4680131/
https://www.ncbi.nlm.nih.gov/pubmed/26220467
http://dx.doi.org/10.1136/jmedgenet-2015-103194
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